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ω-3 脂肪酸通过改善 BPF 诱导的甲状腺功能障碍来保护睾丸功能:p53/Bcl-2 信号和质子泵活性的作用。

Omega 3 fatty acids preserve testicular function by ameliorating BPF-induced dysthyroidism: role of p53/Bcl-2 signaling and proton pump activities.

机构信息

Department of Physiology, University of Ilorin, Ilorin, Nigeria.

Department of Physiology, Federal University of Health Sciences, Ila Orangun, Nigeria.

出版信息

JBRA Assist Reprod. 2024 Aug 26;28(3):471-482. doi: 10.5935/1518-0557.20240033.

Abstract

OBJECTIVE

Bisphenol F (BPF) is an endocrinedisrupting chemical, but information about its effect on thyroid hormones has not been fully explored. Omega 3 fatty acids (O3FA), on the other hand, are antioxidant and antiapoptotic agents. Therefore, this study explored the role and associated molecular mechanism of O3FA in BPF-induced hypothyroidism-mediated testicular dysfunction in male Wistar rats.

METHODS

Twenty (20) male Wistar rats were randomized into four groups (n=5/group), namely: the control group; the BPF treated group (30 mg/kg of BPF); and the intervention groups (30mg/kg BPF + 100mg/kg O3FA (BPF+O3FA-L) and 30mg/kg BPF + 300mg/kg of O3FA for 28 days).

RESULTS

Low and high doses of O3FA ameliorated BPF-induced hypothyroidism-mediated reduction in sperm quality, testosterone, luteinizing hormone, follicle-stimulating hormone, catalase, superoxide dismutase, total antioxidant capacity, and nuclear factor erythroid 2-related factor 2 and increases in estrogen, malondialdehyde, c-reactive protein, interleukin 1 beta, caspase 3. Furthermore, O3FA prevented BPF-induced Na+/K+-ATPase and Ca2+-ATPase dysfunction, estrogen receptor beta overexpression, and tumor protein P53 (p53)/ b-cell lymphoma 2 (Bcl-2) imbalance.

CONCLUSIONS

This study showed that O3FA ameliorated BPF-induced dysthyroidism-mediated testicular dysfunction by preventing proton pump dysfunction and p53/BCl-2 imbalance.

摘要

目的

双酚 F(BPF)是一种内分泌干扰化学物质,但关于其对甲状腺激素影响的信息尚未得到充分探索。另一方面,ω-3 脂肪酸(O3FA)是抗氧化剂和抗凋亡剂。因此,本研究探讨了 O3FA 在 BPF 诱导的甲状腺功能减退介导的雄性 Wistar 大鼠睾丸功能障碍中的作用及其相关分子机制。

方法

将 20 只雄性 Wistar 大鼠随机分为四组(每组 5 只),即:对照组;BPF 处理组(30mg/kg BPF);干预组(30mg/kg BPF+100mg/kg O3FA(BPF+O3FA-L)和 30mg/kg BPF+300mg/kg O3FA,持续 28 天)。

结果

低剂量和高剂量的 O3FA 改善了 BPF 诱导的甲状腺功能减退介导的精子质量、睾酮、促黄体生成素、促卵泡生成素、过氧化氢酶、超氧化物歧化酶、总抗氧化能力和核因子红细胞 2 相关因子 2 降低,以及雌激素、丙二醛、C-反应蛋白、白细胞介素 1β、半胱氨酸天冬氨酸蛋白酶 3 升高。此外,O3FA 防止了 BPF 诱导的 Na+/K+-ATP 酶和 Ca2+-ATP 酶功能障碍、雌激素受体β过表达以及肿瘤蛋白 P53(p53)/B 细胞淋巴瘤 2(Bcl-2)失衡。

结论

本研究表明,O3FA 通过防止质子泵功能障碍和 p53/Bcl-2 失衡,改善了 BPF 诱导的甲状腺功能减退介导的睾丸功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab2c/11349269/831b05ad628f/jbra-28-03-0471-g01.jpg

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